dc.contributor.author |
Maruapula, Dorcas
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|
dc.contributor.author |
Ditshwanelo, Doreen
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|
dc.contributor.author |
Pema, Marea N.
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|
dc.contributor.author |
Bareng, Ontlametse T.
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|
dc.contributor.author |
Choga, Wonderful T.
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|
dc.contributor.author |
Moraka, Natasha O.
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dc.contributor.author |
Mokgethi, Patrick T.
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dc.contributor.author |
Seatla, Kaelo K.
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|
dc.contributor.author |
Koofhethile, Catherine K.
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dc.contributor.author |
Zuze, Boitumelo
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dc.contributor.author |
Gaolathe, Tendani
|
|
dc.contributor.author |
Pretorius-Holme, Molly
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|
dc.contributor.author |
Lebani, Kebaneilwe
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|
dc.contributor.author |
Makhema, Joseph
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dc.contributor.author |
Novitsky, Vlad
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dc.contributor.author |
Shapiro, Roger
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|
dc.contributor.author |
Lockman, Shahin
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dc.contributor.author |
Moyo, Sikhulile
|
|
dc.contributor.author |
Gaseitsiwe, Simani
|
|
dc.date.accessioned |
2024-12-04T05:36:23Z |
|
dc.date.available |
2024-12-04T05:36:23Z |
|
dc.date.issued |
2024-10 |
|
dc.description |
DATA AVAILABITY STATEMENT: Publicly available datasets were analyzed in this study. This
data can be found here: HIV-1 sequences are available on request
through the PANGEA consortium (www.pangea-hiv.org). BCPP
data are available at https://data.cdc.gov/Global-Health/BotswanaCombination-Prevention-Project-BCPP-Publi/qcw5-4m9q. |
en_US |
dc.description.abstract |
BACKGROUND: We evaluated the prevalence of archived proviral drug resistance
mutations (DRMs) associated with resistance to integrase strand transfer
inhibitors (INSTIs) shortly before Botswana transitioned in 2016 to using
dolutegravir (DTG)-based antiretroviral treatment in first-line regimens.
METHODS: We used the Stanford University HIV drug resistance database to
analyze INSTI-resistance associated mutations (RAMs) in a large representative
population-based cohort of adults recruited in 30 geographically dispersed
communities as part of the Botswana Combination Prevention Project (BCPP)
cohort from 2013 to 2018. A total of 5,144 HIV-1 proviral DNA sequences were
included in our analysis; 1,281 sequences were from antiretroviral therapy
(ART)-naïve individuals and 3,863 sequences were from non-nucleoside
reverse transcriptase inhibitor (NNRTI) ART-experienced individuals. None of
the sequences were from DTG-ART experienced participants.
RESULTS: The overall prevalence of major INSTIs DRMs was 1.11% (95% CI
0.82–1.39%). The prevalence of INSTI DRMs in ART-naïve individuals was
1.64% (21/1,281) and 0.93% (36/3,863) in ART-experienced individuals. Major
INSTI-RAMs detected in ART-naïve individuals were E138K (2/1,281; 0.16%),
G140R (8/1,281;0.62%), E92G (2/1,281;0.16%), R263K (5/1,281; 0.4%), N155H
(1/1,281; 0.08%), P145S (1/1,281;0.008%). Among the ART-experienced
individuals, major INSTI RAMs detected were E138K (4/3,863; 0.10%), G140R
(25/3,863;0.65%), G118R (2/3,863, 0.05%), R263K (4/3,863, 0.10%), T66I (1/3,863;0.03%), E138K + G140R (1/3,863, 0.03%|), G140R + R263K (1/3,863,
0.03%). High-level resistance to cabotegravir (CAB), elvitegravir (EVG), and
raltegravir (RAL) was detected in 0.70, 0.16 and 0.06% of the individuals,
respectively. Notably, bictegravir (BIC) and dolutegravir (DTG) showed no
high-level resistance.
CONCLUSION: The overall prevalence of archived INSTI RAMs in Botswana was low
prior to transitioning to first-line DTG-based ART regimens, and did not differ
between ART-naïve and ART-experienced individuals. Ongoing surveillance of
INSTI DRMs in Botswana will allow for re-assessment of INSTI resistance risk
following nationwide DTG rollout. |
en_US |
dc.description.department |
School of Health Systems and Public Health (SHSPH) |
en_US |
dc.description.sdg |
SDG-03:Good heatlh and well-being |
en_US |
dc.description.sponsorship |
The President’s Emergency Plan for AIDS Relief, the Sub-Saharan African Network for TB/HIV Research Excellence from the Bill & Melinda Gates Foundation, the Fogarty International Center at the US National Institutes of Health Award, the Fogarty International Center at the US National Institutes of Health Award, the European Union, the Trials of Excellence in Southern Africa, Africa Research Excellence Fund Research Development Fellowship. |
en_US |
dc.description.uri |
https://www.frontiersin.org/journals/microbiology |
en_US |
dc.identifier.citation |
Maruapula, D., Ditshwanelo, D., Pema, M.N., Bareng, O.T., Choga, W.T., Moraka, N.O., Mokgethi, P.T., Seatla, K.K., Koofhethile, C.K., Zuze, B.J., Gaolathe, T., Pretorius-Holme, M., Lebani, K., Makhema, J., Novitsky, V., Shapiro, R., Lockman, S.., Moyo, S. & Gaseitsiwe, S. (2024) Low prevalence of archived integrase
strand transfer inhibitors resistance associated
mutations in Botswana before the roll out of
dolutegravir based first line antiretroviral
therapy. Frontiers in Microbiology 15:1482348.
doi: 10.3389/fmicb.2024.1482348 |
en_US |
dc.identifier.issn |
1664-302X (online) |
|
dc.identifier.other |
10.3389/fmicb.2024.1482348 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/99737 |
|
dc.language.iso |
en |
en_US |
dc.publisher |
Frontiers Media |
en_US |
dc.rights |
© 2024 Maruapula, Ditshwanelo, Pema,
Bareng, Choga, Moraka, Mokgethi, Seatla,
Koofhethile, Zuze, Gaolathe,
Pretorius-Holme, Lebani, Makhema, Novitsky,
Shapiro, Lockman, Moyo and Gaseitsiwe. This
is an open-access article distributed under
the terms of the Creative Commons
Attribution License (CC BY). |
en_US |
dc.subject |
Botswana |
en_US |
dc.subject |
HIV drug resistance mutations |
en_US |
dc.subject |
SDG-03: Good health and well-being |
en_US |
dc.subject |
Human immunodeficiency virus (HIV) |
en_US |
dc.subject |
Integrase strand transfer inhibitor (INSTI) |
en_US |
dc.subject |
Dolutegravir (DTG) |
en_US |
dc.subject |
Antiretroviral therapy (ART) |
en_US |
dc.title |
Low prevalence of archived integrase strand transfer inhibitors resistance associated mutations in Botswana before the roll out of dolutegravir based first line antiretroviral therapy |
en_US |
dc.type |
Article |
en_US |